Open–Close: An Alternative Strategy to α-Functionalization of Lactone via Enamine Catalysis in One Pot under Mild Conditions-Reference-Cited by-同舟云学术

Open–Close: An Alternative Strategy to α-Functionalization of Lactone via Enamine Catalysis in One Pot under Mild Conditions

Published:2015-04-09 Issue:8 Volume:17 Page:2022-2025
ISSN:1523-7060
Container-title:Organic Letters
language:en
Short-container-title:Org. Lett.

Author:

Liu Yan-Kai¹,Li Zhi-Long²,Li Ji-Yao¹,Feng Huan-Xi¹,Tong Zhi-Ping²

Affiliation:

1. Key Laboratory of Marine Drugs, Chinese Ministry of Education, School of Medicine and Pharmacy, Ocean University of China, Qingdao 266003, P. R. China

2. School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan 610031, P. R. China

Funder

Shandong Province

Ocean University of China

National Natural Science Foundation of China

Publisher

American Chemical Society (ACS)

Subject

Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/acs.orglett.5b00794

Reference50 articles.

1. Natural and Synthetic Chromenes, Fused Chromenes, and Versatility of Dihydrobenzo[h]chromenes in Organic Synthesis

2. Stereoselective Synthesis of Trifluoromethylated Compounds with Controlled Adjacent Tertiary Carbons by Michael Addition to (E)-3-(Trifluoromethyl)acrylates

3. Addition of Ketone and Ester Lithium Enolates to (E)-.beta.-Nitroenones

4. Enantioselective and Diastereoselective Tsuji-Trost Allylic Alkylation of Lactones: An Experimental and Computational Study

5. Highly Stereoselective Aldol Reactions of Lithium Ester Enolates with (RS)-2-(p-Tolylsulfinyl)cyclohexanones

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